@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_head {
  this: np:hasAssertion dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_assertion;
    np:hasProvenance dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_provenance;
    np:hasPublicationInfo dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_assertion a np:Assertion .
  
  dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_provenance a np:Provenance .
  
  dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_assertion {
  miriam-gene:189 a ncit:C16612 .
  
  lld:C0392525 a ncit:C7057 .
  
  dgn-gda:DGN96d409d5004f3d37da689feba192899a sio:SIO_000628 miriam-gene:189, lld:C0392525;
    a sio:SIO_001121 .
}

dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_provenance {
  dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_assertion dcterms:description
      "[The new technology could also be helpful in the search for healthy carriers of AGXT mutations amongst family members and their partners, and for screening of AGXT polymorphisms in patients with nephrolithiasis and healthy populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:11699734;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP252954.RADYm0kBNId0IsTC0Z0NwKWU7L785FFm-vTN6os-X3wgs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:21+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}